A tandem radical cyclization route to tricyclo[4.3.n.0(1,5)]alkanes

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dc.contributor.authorLee, Hee Yoonko
dc.contributor.authorLee, Sko
dc.contributor.authorKim, BGko
dc.contributor.authorBahn, JSko
dc.date.accessioned2013-03-03T15:07:01Z-
dc.date.available2013-03-03T15:07:01Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2004-09-
dc.identifier.citationTETRAHEDRON LETTERS, v.45, no.39, pp.7225 - 7229-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/79165-
dc.description.abstractA facile route to tricyclo[4.3.n.0(1.5)]alkane skeletons from conjugated cyclic enones was developed through tandem free radical cyclization reaction sequence involving the cyclopropylmethyl radical mediated rearrangement. The scope and limitation of the reaction was investigated. (C) 2004 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectREARRANGEMENT-
dc.subjectCONSTRUCTION-
dc.subjectSKELETON-
dc.titleA tandem radical cyclization route to tricyclo[4.3.n.0(1,5)]alkanes-
dc.typeArticle-
dc.identifier.wosid000224017200011-
dc.identifier.scopusid2-s2.0-4444324963-
dc.type.rimsART-
dc.citation.volume45-
dc.citation.issue39-
dc.citation.beginningpage7225-
dc.citation.endingpage7229-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.identifier.doi10.1016/j.tetlet.2004.08.031-
dc.contributor.localauthorLee, Hee Yoon-
dc.contributor.nonIdAuthorLee, S-
dc.contributor.nonIdAuthorKim, BG-
dc.contributor.nonIdAuthorBahn, JS-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorradical-
dc.subject.keywordAuthorcyclization-
dc.subject.keywordAuthormechanism-
dc.subject.keywordPlusREARRANGEMENT-
dc.subject.keywordPlusCONSTRUCTION-
dc.subject.keywordPlusSKELETON-
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